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KIAA0355 (KIAA0355)

Identity

Other alias-
HGNC (Hugo) KIAA0355
LocusID (NCBI) 9710
Atlas_Id 54404
Location 19q13.11  [Link to chromosome band 19q13]
Location_base_pair Starts at 34745456 and ends at 34846471 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
KIAA0355 (19q13.11) / KIAA0355 (19q13.11)KIAA0355 (19q13.11) / UQCRC1 (3p21.31)WTIP (19q13.11) / KIAA0355 (19q13.11)
WTIP 19q13.11 / KIAA0355 19q13.11

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)KIAA0355   29016
Cards
Entrez_Gene (NCBI)KIAA0355  9710  KIAA0355
Aliases
GeneCards (Weizmann)KIAA0355
Ensembl hg19 (Hinxton)ENSG00000166398 [Gene_View]  chr19:34745456-34846471 [Contig_View]  KIAA0355 [Vega]
Ensembl hg38 (Hinxton)ENSG00000166398 [Gene_View]  chr19:34745456-34846471 [Contig_View]  KIAA0355 [Vega]
ICGC DataPortalENSG00000166398
TCGA cBioPortalKIAA0355
AceView (NCBI)KIAA0355
Genatlas (Paris)KIAA0355
WikiGenes9710
SOURCE (Princeton)KIAA0355
Genetics Home Reference (NIH)KIAA0355
Genomic and cartography
GoldenPath hg19 (UCSC)KIAA0355  -     chr19:34745456-34846471 +  19q13.11   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)KIAA0355  -     19q13.11   [Description]    (hg38-Dec_2013)
EnsemblKIAA0355 - 19q13.11 [CytoView hg19]  KIAA0355 - 19q13.11 [CytoView hg38]
Mapping of homologs : NCBIKIAA0355 [Mapview hg19]  KIAA0355 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB002353 AK311350 AU100313 BC017790 BC104761
RefSeq transcript (Entrez)NM_014686
RefSeq genomic (Entrez)NC_000019 NC_018930 NT_011109 NT_187619 NW_003315963 NW_004929415
Consensus coding sequences : CCDS (NCBI)KIAA0355
Cluster EST : UnigeneHs.330073 [ NCBI ]
CGAP (NCI)Hs.330073
Alternative Splicing GalleryENSG00000166398
Gene ExpressionKIAA0355 [ NCBI-GEO ]   KIAA0355 [ EBI - ARRAY_EXPRESS ]   KIAA0355 [ SEEK ]   KIAA0355 [ MEM ]
Gene Expression Viewer (FireBrowse)KIAA0355 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9710
GTEX Portal (Tissue expression)KIAA0355
Protein : pattern, domain, 3D structure
UniProt/SwissProtO15063   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO15063  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO15063
Splice isoforms : SwissVarO15063
PhosPhoSitePlusO15063
Domains : Interpro (EBI)DUF4745   
Domain families : Pfam (Sanger)DUF4745 (PF15923)   
Domain families : Pfam (NCBI)pfam15923   
Conserved Domain (NCBI)KIAA0355
DMDM Disease mutations9710
Blocks (Seattle)KIAA0355
SuperfamilyO15063
Human Protein AtlasENSG00000166398
Peptide AtlasO15063
HPRD11077
IPIIPI00004527   IPI01013704   
Protein Interaction databases
DIP (DOE-UCLA)O15063
IntAct (EBI)O15063
FunCoupENSG00000166398
BioGRIDKIAA0355
STRING (EMBL)KIAA0355
ZODIACKIAA0355
Ontologies - Pathways
QuickGOO15063
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkKIAA0355
Atlas of Cancer Signalling NetworkKIAA0355
Wikipedia pathwaysKIAA0355
Orthology - Evolution
OrthoDB9710
GeneTree (enSembl)ENSG00000166398
Phylogenetic Trees/Animal Genes : TreeFamKIAA0355
HOVERGENO15063
HOGENOMO15063
Homologs : HomoloGeneKIAA0355
Homology/Alignments : Family Browser (UCSC)KIAA0355
Gene fusions - Rearrangements
Fusion : MitelmanKIAA0355/UQCRC1 [19q13.11/3p21.31]  
Fusion : MitelmanWTIP/KIAA0355 [19q13.11/19q13.11]  [t(19;19)(q13;q13)]  
Fusion: TCGAWTIP 19q13.11 KIAA0355 19q13.11 BRCA
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerKIAA0355 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)KIAA0355
dbVarKIAA0355
ClinVarKIAA0355
1000_GenomesKIAA0355 
Exome Variant ServerKIAA0355
ExAC (Exome Aggregation Consortium)KIAA0355 (select the gene name)
Genetic variants : HAPMAP9710
Genomic Variants (DGV)KIAA0355 [DGVbeta]
DECIPHER (Syndromes)19:34745456-34846471  ENSG00000166398
CONAN: Copy Number AnalysisKIAA0355 
Mutations
ICGC Data PortalKIAA0355 
TCGA Data PortalKIAA0355 
Broad Tumor PortalKIAA0355
OASIS PortalKIAA0355 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICKIAA0355  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDKIAA0355
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch KIAA0355
DgiDB (Drug Gene Interaction Database)KIAA0355
DoCM (Curated mutations)KIAA0355 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)KIAA0355 (select a term)
intoGenKIAA0355
Cancer3DKIAA0355(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenKIAA0355
Genetic Testing Registry KIAA0355
NextProtO15063 [Medical]
TSGene9710
GENETestsKIAA0355
Huge Navigator KIAA0355 [HugePedia]
snp3D : Map Gene to Disease9710
BioCentury BCIQKIAA0355
ClinGenKIAA0355
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9710
Chemical/Pharm GKB GenePA134927016
Clinical trialKIAA0355
Miscellaneous
canSAR (ICR)KIAA0355 (select the gene name)
Probes
Litterature
PubMed10 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineKIAA0355
EVEXKIAA0355
GoPubMedKIAA0355
iHOPKIAA0355
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Mar 30 15:06:05 CEST 2017

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